US11123523B2 - Intravenous catheter device with integrated extension tube - Google Patents

Abstract

The present invention relates to peripheral intravenous catheters, and in particular to an integrated peripheral intravenous catheter having a low profile securement platform, a needle hub having an interior compartment and further comprising a paddle grip, and an extension tube coupled to the catheter and stored within the interior compartment of the needle hub prior to catheterization.

Description

RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 15/286,281, filed Oct. 5, 2016, and entitled INTRAVENOUS CATHETER DEVICE WITH INTEGRATED EXTENSION TUBE, which claims the benefit of U.S. Provisional Patent Application No. 62/247,599, which was filed Oct. 28, 2015, U.S. Provisional Patent Application No. 62/247,596, which was filed on Oct. 28, 2015, U.S. Provisional Patent Application No. 62/296,383, which was filed on Feb. 17, 2016, U.S. Provisional Patent Application No. 62/247,617, which was filed on Oct. 28, 2015, U.S. Provisional Patent Application Ser. No. 62/247,607, which was filed Oct. 28, 2015, U.S. Provisional Patent Application Ser. No. 62/247,621, which was filed Oct. 28, 2015, U.S. Provisional Patent Application Ser. No. 62/247,624, which was filed Oct. 28, 2015, U.S. Provisional Application No. 62/247,626, which was filed on Oct. 28, 2015, and U.S. Provisional Application No. 62/296,385, which was filed on Feb. 17, 2016, each of which is incorporated herein by reference in their entirety.

BACKGROUND OF THE INVENTION

In medicine, an intravenous is a catheter placed into a peripheral vein in order to administer medications or fluids to a patient in need. An intravenous catheter may also be used to draw blood.

The catheter is introduced into the patient's vein by an introducer needle that is positioned within the lumen of the catheter, such that a sharpened tip of the needle is exposed beyond the distal tip of the catheter. The sharpened tip punctures the skin and vein of the patient to provide a pathway through which the distal tip of the catheter may be advanced. Once the catheter tip is placed into the vein, the needle tip is withdrawn into the catheter; a technique commonly referred to as “hooding”. The catheter and needle are then advanced into the vein to a desired depth, after which the needle is entirely removed from the catheter. The catheter is then secured to the patient's skin by an adhesive strip or wrapping.

Generally a catheter is coupled to a catheter adapter having a blood control device, such as a valve or septum. As such, blood flowing through the catheter is retained within the catheter adapter until the blood control device is actuated or otherwise manipulated to permit flow through the catheter and catheter adapter.

An extension tube generally comprises a flexible section of tubing having a first end that is configured to compatibly couple to a catheter or catheter adapter, and further comprises a second end that may be accessed directly by a syringe or needle, or may be further coupled to an intravenous bag by a section of intravenous tubing. As a common practice, an extension tube is coupled to the catheter adapter following placement of the catheter. In some instances, a clinician may be required to manually occlude the patient's vein and/or the catheter while simultaneously attaching an extension tube thereto. In other instances, a clinician must take care to immobilize the catheter and/or catheter adapter while attaching the extension tube to prevent accidental removal of the inserted catheter. Further, in many instances a clinician is required to sterilize the mating ends of the catheter adapter and the extension tube prior to making the connection, thus adding an additional step to the procedure.

Thus, although methods and devices currently exist for accessing the vasculature of a patient via a catheter and an extension tube, challenges still remain. Accordingly, the features of the present invention address and overcome these challenges.

BRIEF SUMMARY OF THE INVENTION

The present invention relates to peripheral intravenous catheters, and in particular to an integrated peripheral intravenous catheter having a low profile securement platform, a needle hub having an interior compartment and further comprising a paddle grip, and an extension tube coupled to the catheter and stored within the interior compartment of the needle hub prior to insertion of the catheter.

Some implementations of the present invention comprise an intravenous catheter device having a catheter adapter having a proximal end, a distal end, and a lumen interposed therebetween. The catheter adapter further comprises a securement platform that is constructed of a soft, pliable or flexible material, such as a soft polymer. In some instances, the securement platform comprises a soft, polymer material comprising a Shore A durometer hardness of from approximately 15 to 100. In some instances, the soft, polymer material comprises a durometer hardness of from approximately 30 Shore A to approximately 90 Shore D. In some instances, the soft, polymer material comprises a durometer hardness of from approximately 50 Shore A to approximately 90 Shore D. In some instances, the distal end of the catheter adapter comprises an intravenous catheter in fluid communication with the lumen. Further, the proximal end of the catheter adapter comprises an extension tube that is also in fluid communication with the lumen. In some instances, securement platform may further comprise a hard or rigid plastic polymer material.

Some implementations of the present invention further comprise a needle hub comprising a rigid material, such as a hard plastic material. The needle hub comprises an open end, a closed end, and a compartment interposed therebetween. The closed end is configured to receive a terminal end of the extension tube, and the open end is configured to receive the proximal end of the catheter adapter, wherein the extension tube is stored within the compartment. In some instances, the extension tube is wound around an outer surface of the needle hub. In some instances, the closed end further comprises a flashback chamber in fluid communication with an interior lumen of the introducer needle.

In some instances, the needle hub further comprises a paddle grip positioned in proximity to the open end and arranged to overlap the securement platform, thereby permitting the user to pinch the paddle grip and securement platform between their thumb and index finger during the process of catheterization. In some instances, the overlapping arrangement of the paddle grip and the securement platform permits the user to hood the tip end of the needle by adjusting their grip to move the securement platform and paddle grip in opposite directions.

The needle hub further comprises an introducer needle having a base end, a tip end, and a body extending therebetween. The base end of the needle is securely attached to the closed end of the needle hub. When assembled, the body of the needle extends outwardly from the closed end, through the proximal end, the lumen, the distal end, and the intravenous catheter, such that the tip end of the needle is exposed beyond a terminal end of the intravenous catheter.

Some implementations of the present invention are further configured such that the body of the introducer needle passes through an interior of the extension tube when the intravenous catheter device is assembled. In some instances, the extension tube is wound around the body of the introducer needle within the compartment.

In some instances, the proximal end of the catheter adapter, and/or the terminal end of the extension tube further comprises a blood control device, such as a valve, a self-sealing polymer, a luer adapter, or a septum. In some instances, the blood control valve comprises a passageway through which the body of the introducer needle passes. In some instances, the blood control device is a single-use device. In other instances, the blood control device is a multi-use device.

Some implementations of the present invention further comprise an extension tube having an access port that is coupled to a sidewall surface of the extension tube, and extending outwardly therefrom. For these embodiments, the needle hub further comprises an access slot extending proximally from the open end to a position that is in proximity to the closed end, whereby the access port passes through the access slot and is located externally to the compartment of the needle hub with the intravenous catheter device is assembled. In some instances, the open end of the needle hub further comprises a notch having a width and depth that is configured to receive and support a proximal edge of the securement platform of the catheter adapter.

Some implementations of the present invention further comprise one or more features designed to capture and shield the tip end of the introducer needle following catheterization of the patient. For example, in some instances the proximal end of the extension tube further comprises a needle shield or safety mechanism that is selectively coupled thereto and through which the body of the introducer needle passes when the device is assembled. Upon removal of the introducer needle from the extension tube, a needle feature, such as a ferrule or notch, actuates the safety mechanism to selectively disengage the safety mechanism from the terminal end of the extension tube. Once released, the safety mechanism captures the tip end of the needle, thereby preventing unintended exposure to the tip end of the needle.

This summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description. This Summary is not intended to identify key features or essential features of the claimed subject matter, nor is it intended to be used as an aid in determining the scope of the claimed subject matter.

Additional features and advantages of the invention will be set forth in the description which follows, and in part will be obvious from the description, or may be learned by the practice of the invention. The features and advantages of the invention may be realized and obtained by means of the instruments and combinations particularly pointed out in the appended claims. These and other features of the present invention will become more fully apparent from the following description and appended claims, or may be learned by the practice of the invention as set forth hereinafter.

BRIEF DESCRIPTION OF THE DRAWINGS

In order to describe the manner in which the above-recited and other advantages and features of the invention can be obtained, a more particular description of the invention briefly described above will be rendered by reference to specific embodiments thereof which are illustrated in the appended drawings. Understanding that these drawings depict only typical embodiments of the invention and are not therefore to be considered to be limiting of its scope, the invention will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:

FIG. 1A is a perspective top view of an assembled intravenous catheter device in accordance with a representative embodiment of the present invention.

FIG. 1B illustrates a perspective top view of an intravenous catheter device that includes an example nested securement platform in accordance with a representative of the present invention.

FIG. 1C is an upper perspective view of an example paddle grip of the intravenous catheter device ofFIG. 1B in accordance with a representative embodiment of the present invention.

FIG. 2 is a cross-sectioned top view of an assembled intravenous catheter device in accordance with a representative embodiment of the present invention.

FIG. 3 is an exploded, cross-section top view of an intravenous catheter device in accordance with a representative embodiment of the present invention.

FIG. 4A is a cross-sectioned top view of an assembled intravenous catheter device having an access line in accordance with a representative embodiment of the present invention.

FIG. 4B is a perspective top view of an assembled intravenous catheter device that includes an example nested securement platform in accordance with a representative of the present invention.

FIG. 5 is a perspective side view of the disassembled intravenous catheter device ofFIG. 4A in accordance with a representative embodiment of the present invention.

FIG. 6A is cross-sectioned top view of an assembled intravenous catheter device in accordance with a representative embodiment of the present invention.

FIG. 6B is a cross-sectioned side view of an assembled intravenous catheter device in accordance with a representative embodiment of the present invention.

FIG. 6C is a cross-sectioned top view of a catheter adapter and extension tube following removal of the introducer needle and needle hub in accordance with a representative embodiment of the present invention.

FIG. 7 is a cross-sectioned top view of an intravenous catheter device having second cannula fixedly secured within the catheter and configured to receive the outer diameter of the introducer needle in accordance with a representative embodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to peripheral intravenous catheters, and in particular to an integrated peripheral intravenous catheter having a low profile securement platform, a needle hub having an interior compartment and further comprising a paddle grip, and an extension tube coupled to the catheter and stored within the interior compartment of the needle hub prior to insertion of the catheter.

Some implementations of the present invention comprise an intravenous catheter device having a catheter adapter having a proximal end, a distal end, and a lumen interposed therebetween. The catheter adapter further comprises a securement platform that is constructed of a soft, pliable or flexible material, such as a soft polymer. In some instances, the securement platform comprises a soft, polymer material comprising a Shore A durometer hardness of from approximately 15 to 100. In some instances, the soft, polymer material comprises a durometer hardness of from approximately 30 Shore A to approximately 90 Shore D. In some instances, the soft, polymer material comprises a durometer hardness of from approximately 50 Shore A to approximately 90 Shore D. In some instances, the distal end of the catheter adapter comprises an intravenous catheter in fluid communication with the lumen. Further, the proximal end of the catheter adapter comprises an extension tube that is also in fluid communication with the lumen. In some instances, securement platform may further comprise a hard or rigid plastic polymer material.

Some implementations of the present invention further comprise a needle hub comprising a rigid material, such as a hard plastic material. The needle hub comprises an open end, a closed end, and a compartment interposed therebetween. The closed end is configured to receive a terminal end of the extension tube, and the open end is configured to receive the proximal end of the catheter adapter, wherein the extension tube is stored within the compartment. In some instances, the extension tube is wound around an outer surface of the needle hub. In some instances, the closed end further comprises a flashback chamber in fluid communication with an interior lumen of the introducer needle.

In some instances, the needle hub further comprises a paddle grip positioned in proximity to the open end and arranged to overlap the securement platform, thereby permitting the user to pinch the paddle grip and securement platform between their thumb and index finger during the process of catheterization. In some instances, the overlapping arrangement of the paddle grip and the securement platform permits the user to hood the tip end of the needle by adjusting their grip to move the securement platform and paddle grip in opposite directions.

The needle hub further comprises an introducer needle having a base end, a tip end, and a body extending therebetween. The base end of the needle is securely attached to the closed end of the needle hub. When assembled, the body of the needle extends outwardly from the closed end, through the proximal end, the lumen, the distal end, and the intravenous catheter, such that the tip end of the needle is exposed beyond a terminal end of the intravenous catheter.

Some implementations of the present invention are further configured such that the body of the introducer needle passes through an interior of the extension tube when the intravenous catheter device is assembled. In some instances, the extension tube is wound around the body of the introducer needle within the compartment.

In some instances, the proximal end of the catheter adapter, and/or the terminal end of the extension tube further comprises a blood control device, such as a valve, a self-sealing polymer, a luer adapter, or a septum. In some instances, the blood control valve comprises a passageway through which the body of the introducer needle passes. In some instances, the blood control device is a single-use device. In other instances, the blood control device is a multi-use device.

Some implementations of the present invention further comprise an extension tube having an access port that is coupled to a sidewall surface of the extension tube, and extending outwardly therefrom. For these embodiments, the needle hub further comprises an access slot extending proximally from the open end to a position that is in proximity to the closed end, whereby the access port passes through the access slot and is located externally to the compartment of the needle hub with the intravenous catheter device is assembled. In some instances, the open end of the needle hub further comprises a notch having a width and depth that is configured to receive and support a proximal edge of the securement platform of the catheter adapter.

Some implementations of the present invention further comprise one or more features designed to capture and shield the tip end of the introducer needle following catheterization of the patient. For example, in some instances the proximal end of the extension tube further comprises a needle shield or safety mechanism that is selectively coupled thereto and through which the body of the introducer needle passes when the device is assembled. Upon removal of the introducer needle from the extension tube, a needle feature, such as a ferrule or notch, actuates the safety mechanism to selectively disengage the safety mechanism from the terminal end of the extension tube. Once released, the safety mechanism captures the tip end of the needle, thereby preventing unintended exposure to the tip end of the needle.

With reference toFIGS. 1 and 2, perspective top and cross-sectioned views of an assembledintravenous catheter device10 are illustrated. In some embodiments,catheter device10 comprises acatheter adapter20 having aproximal end22, adistal end24, and alumen26 extending therebetween.Distal end24 further comprises anintravenous catheter30 having a gauge configured to access the peripheral vascular system.

Catheter adapter20 further comprises one ormore securement platforms40. In some embodiments,securement platforms40 comprise a soft, pliable polymer material that may easily conform to the contours of the patient's body in proximity to the catheter insertion site, thus providing a low profile securement platform. In some instances,securement platforms40 comprise a soft polymer material having a Shore A durometer hardness of from approximately 15 to 100, from approximately 20 to 80, from approximately 30 to 70, from approximately 40 to 60, from approximately 45 to 55, or approximately 50. In some instances, a soft, polymer material comprises a Shore A durometer hardness of less than 15. In some instances, a soft, polymer material comprises a Shore A durometer hardness of greater than 100. In some instances, bothcatheter adapter20 andsecurement platform40 comprise a soft, pliable polymer material.

Proximal end22 ofcatheter adapter20 further comprises anextension tube50 having afirst end52 coupled toproximal end22, and further comprises adistal end54 having ablood control device56. In some instances,extension tube50 andcatheter30 comprise a single, monolithic structure or component. In other instances,extension tube50 andcatheter30 are separate devices or components that are each independently coupled tolumen26, such thatextension tube50,catheter30, andlumen26 are in fluid communication. In some instances,lumen26 further comprises a blood control device, such as a one-way valve or septum (not shown).

In some embodiments, the septum may have a “low friction” or “low drag” design configured to provide relatively low resistance to withdrawal of anintroducer needle70 proximally through the septum, which occurs as thecatheter device10 transitions from an insertion configuration to a fluid delivery configuration. The resistance to withdrawal of theneedle70 through the septum may be sufficiently low that the clinician can relatively easily move thecatheter device10 from the insertion configuration to the fluid delivery configuration with only a single hand. In some embodiments, the resistance to withdrawal may be, on average, less than about 50 gf.

In some instances, a proximal end ofcatheter adapter20 is extended proximally (not shown) to provideextension tube50. Thus, the proximal end ofcatheter30 terminates within thelumen26 ofcatheter adapter20, andextension tube50 extends outwardly fromcatheter adapter20, whereincatheter30,lumen26, andextension tube50 are in fluid communication. In some instances, a portion ofsecurement platform40 is extended (not shown) to provideextension tube50.

In some embodiments,blood control device56 comprises a luer adapter configured to compatibly receive a luer connector coupled to a length of intravenous tubing, or provide access via a needle or syringe. In some instancesblood control device56 further comprises a valve, the septum, and/or a self-healing polymer that permits selective access to the interior lumen ofextension tube50. In some instances,blood control device56 comprises a single-use valve. In other instances,blood control device56 comprises a multi-use valve.Blood control device56 may further comprise a septum actuator configured for use with a single-use or multi-use valve. When not accessed,blood control device56 retains fluids withincatheter30,catheter adapter20, andextension tube50.

Catheter device10 further comprises aneedle hub60.Needle hub60 comprises aclosed end62, anopen end64, and acompartment66 interposed therebetween.Closed end62 is the proximal-most end ofcatheter device10 and is configured to receive aterminal end54 ofextension tube50.Open end64 is located opposite ofclosed end62 and is configured to compatibly receiveproximal end22 ofcatheter adapter20. In some instances,compartment66 comprises a length sufficient to receive the entire length ofextension tube50. For example, in oneembodiment compartment66 comprises a length from approximately 0.5 inches to approximately 8 inches, from approximately 1 inch to approximately 7.5 inches, from approximately 2 inches to approximately 7 inches, from approximately 3 inches to approximately 6 inches, from approximately 4 inches to approximately 5 inches, or approximately 4.5 inches. In one embodiment,compartment66 is approximately 4 inches.

Catheter device10 further comprises theintroducer needle70.Introducer needle70 comprises a hollow metal or rigid plastic cannula having abase end72 that is securely attached toclosed end62 withincompartment66.Needle70 further comprises a sharpenedtip end74 that is oppositebase end72. Thebody76 ofneedle70 has a length that is greater than the combined lengths ofcatheter adapter20,catheter30, andneedle hub60, when assembled, such thattip end74 is exposed distally beyond aterminal end32 ofcatheter30. As such,tip end74 is exposed and capable of providing access through the patient's skin to introducecatheter30 into the patient's vein.

In some embodiments,introducer needle70 is threaded throughextension tube50,lumen26, andcatheter30 prior to catheterization. In this way,introducer needle70 aligns and coordinates the relative positions of each of the various components.

Various embodiments of the present invention further comprise asafety mechanism80 configured to secure the sharpened,distal tip74 of theintroducer needle70 following removal and separation of theneedle hub60 from thecatheter adapter20. A safety mechanism may include any compatible device known in the art. In some instances, the safety mechanism is configured to interact with a needle feature, such as a ferrule, notch, crimp or bump on the cannula. The crimp or bump formed in the cannula cause a slight out of round configuration that can be used to activate a safety mechanism. In some instance, the safety mechanism comprises an arm or lever that is actuated to capture the needle tip within the mechanism and prevent the tip from emerging prior to safe disposal.

The safety mechanism is attached to the body of the needle and is capable of sliding along the length thereof. In some instances, an initial or assembled position of the safety mechanism is located in proximity to the base or proximal end of the needle adapter prior to catheterization. For some configurations, the assembled position of the safety mechanism is between the proximal end of the needle hub and the proximal end of the catheter adapter or securement platform, wherein the safety mechanism does not overlap the catheter adapter or securement platform. In some instances, a portion of the safety mechanism is positioned within the catheter adapter, with the balance of the safety mechanism being positioned external to the catheter adapter, such as within the needle hub. In some embodiments, a portion of the catheter adapter or securement platform is extended proximally to provide a housing in which at least a portion of the safety mechanism is house. In some instance, the entire safety mechanism is housed within the housing of the catheter adapter or securement platform prior to catheterization.

In some embodiments, the assembled position of the safety mechanism positions the proximal end of the catheter adapter between the distal end of the safety mechanism and a distal end of a paddle grip of the needle hub. In some instances, the assembled position of the safety mechanism positions the proximal end of the catheter adapter between the distal end of the safety mechanism and a proximal end of a paddle grip of the needle hub. In some instances, a portion of the safety mechanism overlaps a portion of a paddle grip of the needle hub. In some embodiments, at least some portion of at least one of the catheter adapter and the paddle grip overlaps at least some portion of the safety mechanism. In some embodiments, no portion of the catheter adapter or paddle grip overlaps any portion of the safety mechanism.

In some embodiments, a defeatable mechanical connection is provided between the safety mechanism and at least one other component of the intravenous catheter device. In some embodiments, a distal end of the safety mechanism is selectively coupled to a proximal end of the catheter adapter. In one embodiment, the safety mechanism interlocks internally to the proximal end of the catheter adapter. In one embodiment, the safety mechanism interlocks externally to the proximal end of the catheter adapter. In some embodiments, a distal end of the safety mechanism is selectively coupled to a proximal end of the securement platform. In some embodiments, a surface of the safety mechanism is selectively coupled to at least one surface of at least one of the catheter adapter, a blood control valve, an extension tube, and the securement platform. In some instances, the mechanical connection is defeated upon securement of the needle tip within the safety mechanism.

In some embodiments,catheter device10 comprises asafety mechanism80 through withbody76 ofneedle70 is threaded, and which is interposedly positioned betweenterminal end54 andclosed end62. Following catheterization and withdrawal ofneedle70 fromextension tube50, aneedle feature78 interacts withsafety mechanism80 to traptip end74 therein, thereby preventing accidental exposure to tipend74. Any combination of known needle feature and safety mechanism may be used within the scope of the present invention.

Needle hub60 further comprises apaddle grip68 positioned in proximity to openend64 and arranged to overlap a portion ofsecurement platform40 whencatheter device10 is assembled. In some embodiments, paddlegrip68 comprises a rigid plastic material. The overlapped arrangement ofsecurement platform40 and paddlegrip68 permits a user to holdcatheter device10 by pinching the overlapped features or components. In one embodiment, a user pinches the overlappingpaddle grip68 andsecurement platform40 in order to insert the catheter into a patient. Oncetip end74 andterminal end32 are inserted within the patient's vein, the user may hood tipend74 by adjusting their grip to movepaddle grip68 in aproximal direction90 while either maintaining the position ofsecurement platform40, or by simultaneously movingsecurement platform40 in adistal direction92.

Oncetip end74 is hooded, the user may further advancecatheter30 into the patient's vein to a final insertion depth. In some instances,catheter30 comprises a clear or translucent material through which the user can see, and which provides primary blood flashback to indicate proper insertion ofcatheter30. In some instances,catheter adapter20 and/orneedle hub60 further comprise a clear or translucent material for purposes of blood flashback observation. In some embodiments,needle feature78 comprises a notch which permits blood within the hollow interior ofneedle70 to flow between the outer surface ofneedle70 and the interior ofcatheter30.

In some embodiments,base end72 ofneedle70 is coupled to a secondary flashback chamber (not shown) that is in fluid communication withtip end74 and the hollow interior ofneedle70. For example,closed end62 may further be modified to include a secondary flashback chamber. As such, blood may flow through the hollow interior ofneedle70 and further flow into the secondary flashback chamber to further indicate proper insertion ofcatheter30 prior to separatingneedle hub60 andneedle70 fromcatheter adapter20,catheter30, andextension tube50.

As illustrated inFIGS. 1B and 1C, in some embodiments, thesecurement platform40 may be nested in thepaddle grip68 in the assembled position or insertion configuration. In further detail, in some embodiments, thepaddle grip68 may include aperipheral ridge69 disposed along an outer edge of thepaddle grip68. In some embodiments, theperipheral ridge69 may define a boundary of adistal recess71 of thepaddle grip40. In some embodiments, thesecurement platform40 may be disposed within thedistal recess71 in the insertion configuration. In some embodiments, a curvature of an outer edge of thesecurement platform40 may correspond to a curvature of an inner edge of theperipheral ridge69 such that thesecurement platform40 fits within thedistal recess71 in the insertion configuration.

In some embodiments, theperipheral ridge69 may act as a pull feature. In some embodiments, theperipheral ridge69 may be positioned such that a digit can easily contact an apex and/or a distal side of theperipheral ridge69 to apply proximal pressure on thepaddle grip68. In some embodiments, theperipheral ridge69 may be disposed outward of an outer edge of thesecurement platform40 when theintravenous catheter device10 is in the insertion configuration such that theperipheral ridge69 may be contacted by the digit even when thesecurement platform40 is positioned to overlie thepaddle grip68.

Referring now toFIG. 3, an exploded, cross-sectioned view ofcatheter device10 is shown. In some embodiments,open end64 ofneedle hub60 further comprises anotch61 having a width and depth sufficient to receive and support aproximal edge42 ofsecurement platform40. In some instances, notch61 comprises a depth sufficient to achieve an overlapped arrangement ofsecurement platform40 and paddlegrip68 whenproximal edge42 is fully inserted withinnotch61. In some instances, with width ofnotch61 is slightly greater than the thickness ofsecurement platform40, such thatsecurement platform40 may easily slide withinnotch61, and notch61 maintains the axial position ofcatheter adapter20 withinopen end64, and further provides a buttressing support to the soft, pliable material ofsecurement platform40.

Referring now toFIGS. 4 and 5, some embodiments of the present invention further comprise anaccess port58 comprising afirst end51 coupled to, and in fluid communication withextension tube50, and further comprising asecond end53 extending outwardly fromextension tube50 and comprising ablood control device57.Access port58 may comprise any structure or length within the teachings of the present invention. In some embodiments,access port58 extends outwardly from the side or sidewall ofextension tube50 at an angle to resemble a y-port. In some instances,access port58 extends outwardly in a proximal direction. In other instances,access port58 extends outwardly in a distal direction. In some instances,access port58 is used topre-prime extension tube50 andcatheter30 prior to catheterization.

Blood control device57 may comprise any structure, shape or feature within the teachings of the present invention, or as is commonly known and practiced in the art. Further,blood control device57 may be coupled to any secondary intravenous device, including but not limited to, intravenous extension tubing, a syringe, a needle, a cap, a secondary flash chamber, a y-port adapter, a vial, an IV bag, a valve, and a clamp.

Unlikeblood control device56,blood control device57 is located outsidecompartment66, and therefore may include features that may be incapable of being stored withincompartment66. For example, in one embodimentblood control device57 comprises a y-port. In one embodiment,blood control device57 comprises one or features in common withblood control device56, as discussed previously.Access port58 may further comprise one or more features that may be incompatible for storage withincompartment66. For example, in oneembodiment access port58 comprises a roller clamp, a pinch clamp, or a similar device to control fluid flow therethrough.

In some instances,access port58 is directly coupled toblood control device56. In some embodiments,access port58 extends fromcatheter adapter20. In some embodiments,catheter device10 comprises a first access port coupled to and extending from catheter adapter20 (not shown), and further comprises asecond access port58 that is coupled toextension tube50 orblood control device56.

In some embodiments,needle hub60 further comprises anaccess slot63 extending proximally fromopen end64 toclosed end62 to accommodateaccess port58.Access slot63 generally comprises a length selected to correspond to the position ofaccess port58 whencatheter device10 is assembled.Access port63 further comprises a width that is slightly larger than the outer diameter ofaccess port63, wherebyaccess port63 is able to free slide withinaccess slot63.

As illustrated inFIG. 4B, in some embodiments, thesecurement platform40 may be nested in thepaddle grip68 in the assembled or insertion configuration, similar to the nesting of thesecurement platform40 in thepaddle grip68, illustrated inFIG. 1B.

Referring now toFIGS. 6A-6C, some embodiments of the present invention further comprise acatheter device100 having anelongated extension tube150, wherein the length ofextension tube150 is greater than the length ofcompartment166. In some instances, the excess length ofextension tube150 is wrapped aroundbody76 ofneedle70 to accommodate storage withincompartment166 prior to catheterization. Following catheterization,extension tube150 is unwound fromneedle70 asneedle70 andneedle hub160 are separated and removed fromcatheter adapter120.

In some embodiments,catheter adapter120 comprises alumen126 having adistal end124 and aproximal end122.Distal end124 comprisesintravenous catheter30, as discussed previously. In some embodiments,proximal end122 comprises a first surface to whichfirst end152 ofextension tube150 is coupled and in fluid communication withlumen126.First end152 is coupled toproximal end122 at an off-center position, such as in proximity to the perimeter edge ofproximal end122.

Proximal end122 further comprises a second surface through which needle70 passes. In some instances, the second surface ofproximal end122 is the axial center ofproximal end122. In some embodiments, second surface ofproximal end122 comprises a blood control device, such as septum or self-healing polymer through which needle70 is passed. Upon removal ofneedle70 fromproximal end122, the blood control device prevents fluid from passing through the second surface ofproximal end122, thereby directing fluid flow throughextension tube150 at the first surface ofproximal end122.

Similarly,blood control device156 comprises afirst aperture151 to which is secured thedistal end154 ofextension tube150. In some instances,first aperture151 is located at an off-center position, such as in proximity to the perimeter edge ofblood control device156.Blood control device156 further comprises asecond aperture153 through which needle70 passes. In some instances,second aperture153 is located at the axial center ofblood control device156. Upon catheterization,blood control device156 retains fluid withinextension tube150 until further accessed by a secondary intravenous device, such as a luer connector, a syringe, a needle, or other device.

In some embodiments,needle hub160 comprises a pair of truncated paddle grips168 having slots that receive the proximal edges ofsecurement platforms140. In some instances, the dimensions and shape of paddle grips168 andsecurement platforms140 are configured to accommodate catheterization by pinching these elements between the user's thumb and index finger. In some embodiments, each of thesecurement platforms140 may be nested in one of the paddle grips168 in the assembled position or insertion configuration, similar to the nesting of thesecurement platform40 in thepaddle grip68, illustrated inFIGS. 1B and 4B.

In some instances, the small gauge and extended length ofintroducer needle70 may result in undesirable flexing or bending ofneedle70 during catheterization. Accordingly, in someembodiments catheter device200 comprises a sleeved needle configuration, as shown inFIG. 7. In some instances,catheter30 comprises asecond cannula250 having an inner diameter that is configured to receive the outer diameter ofneedle70.Second cannula250 may comprise a truncated length and be securely fixed within the interior lumen or fluid pathway ofcatheter30. In some instances,second cannula250 is fixed within the portion ofcatheter30 that is located withincatheter adapter220.Second cannula250 therefore acts as a sheath for the portion ofneedle70 located withincatheter adapter220. In some instances,second cannula250 supports and stiffensneedle70 against undesired flexing or bending.

In some instances,catheter device200 comprises a tapered introducer needle (not shown), wherein the base and middle portions of the tapered needle comprises a gauge and thickness that is greater than the gauge of the distal end and tip portion of the needle. The tapered configuration imparts greater stiffness to the proximal and middle portions of the needle, which serve to stiffen the distal and tip portions of the needle, thereby reducing undesired flexing or bending of the needle during catheterization. Further still, in someembodiments catheter device200 comprises an introducer needle having base and middle portions comprising a first gauge, and distal and tip portions comprising a second gauge, wherein the first gauge is greater than the second gauge, and the first gauge imparts stiffness to the second gauge.

In some embodiments, a particular catheter device, such as, for example, the catheter device of any of theFIGS. 1-7, may include a needle safety mechanism. The safety mechanism may include any safety mechanism configured to secure a sharpened, distal tip of an introducer needle when the needle is withdrawn from a catheter of the particular catheter device, preventing accidental needle sticks.

The safety mechanism may be coupled with the particular catheter device in any number of ways. In some embodiments, the safety mechanism may include an internal interlock in which the safety mechanism is coupled with an internal surface of a catheter adapter. Coupling may include threading, fitting, snapping, connecting, attaching, fastening, clipping, hooking, or any other suitable means of coupling. Non-limiting examples of safety mechanisms that include an internal interlock are provided in: U.S. Pat. No. 8,496,623, titled BI-DIRECTIONAL CANNULA FEATURE CAPTURE MECHANISM, filed Mar. 2, 2009; U.S. Pat. No. 9,399,120, titled BI-DIRECTIONAL CANNULA FEATURE CAPTURE MECHANISM, filed Jul. 11, 2013; U.S. Patent Application No. 62/314,262, titled CANNULA CAPTURE MECHANISM, filed Mar. 28, 2016, each of which is herein incorporated by reference in its entirety. In some embodiments, the safety mechanism may include a clip disposed within the catheter adapter, a non-limiting example of which is provided in U.S. Pat. No. 6,117,108, titled SPRING CLIP SAFETY IV CATHETER, filed Jun. 12, 1998, which is herein incorporated by reference in its entirety.

In some embodiments, the safety mechanism may include an external interlock in which the safety mechanism is coupled with an external surface of the catheter adapter. In some embodiments, the safety mechanism may be coupled with an external surface of the catheter adapter and an internal and/or external surface of a needle hub. Coupling may include threading, fitting, snapping, connecting, attaching, fastening, clipping, hooking, or any other suitable means of coupling. Non-limiting examples of safety mechanisms that include an external interlock are provided in U.S. patent application Ser. No. 14/295,953, titled PORTED IV CATHETER HAVING EXTERNAL NEEDLE SHIELD AND INTERNAL BLOOD CONTROL SEPTUM, filed Jun. 4, 2014, which is herein incorporated by reference in its entirety. In some embodiments, the safety mechanism may include a V-clip or a similar clip. A non-limiting example of a V-clip is provided in U.S. patent application Ser. No. 14/295,953, titled PORTED IV CATHETER HAVING EXTERNAL NEEDLE SHIELD AND INTERNAL BLOOD CONTROL SEPTUM, filed Jun. 4, 2014, which is herein incorporated by reference in its entirety. The V-clip may selectively retain a portion of the catheter adapter.

In some embodiments, a defeatable mechanical connection is provided between the safety mechanism and at least one other component of the IV catheter system. In some instances, the mechanical connection is defeated upon securement of the distal tip of the needle within the safety mechanism. In some embodiments, a surface of the safety mechanism is selectively coupled to one or more of the following: the catheter adapter, a blood control valve, an extension tube, and one or more paddle grips.

In some embodiments, the safety mechanism may include a safety barrel, which may be spring-loaded. For example, the safety barrel may be spring loaded as in the BD™ Insyte® Autoguard™ BC shielded protective IV catheter. In some embodiments, the safety mechanism may be passively and/or actively activated. In some embodiments, the safety mechanism may be configured to interact with a needle feature, such as a ferrule, notch, crimp or bump on the needle. In some embodiments, the safety mechanism may include an arm or lever that may be actuated to capture the distal tip within the safety mechanism and prevent the tip from emerging prior to safe disposal. In some embodiments, the safety mechanism may be attached to a body of the needle and may be capable of sliding along the length thereof.

In some embodiments, in an assembled position prior to catheterization, the safety mechanism may be disposed between the catheter adapter and the needle hub. In some embodiments, the catheter adapter and the needle hub may be spaced apart by at least a portion of the safety mechanism in the assembled position prior to catheterization. In some embodiments, in the assembled position prior to catheterization, a proximal end of the catheter adapter may be disposed between a distal end of the safety mechanism and a distal end of a grip of the needle hub, such as, for example, a paddle grip. In some embodiments, in the assembled position prior to catheterization, the proximal end of the catheter adapter body may be disposed between the distal end of the safety mechanism and a proximal end of the grip of the needle hub. In some embodiments, a portion of the safety mechanism may overlap with a portion of the grip of the needle hub. In some embodiments, at least a portion of at least one of the catheter adapter and the grip overlaps at least some portion of the safety mechanism. In some embodiments, no portion of the catheter adapter body or the grip overlaps any portion of the safety mechanism.

The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.

Claims (14)

The invention claimed is:

1. An assembled intravenous catheter device, comprising:

a catheter adapter having a proximal end, a distal end, and a lumen interposed therebetween, the catheter adapter further comprising a securement platform, the distal end of the catheter adapter comprising an intravenous catheter and the proximal end of the catheter adapter comprising an extension tube, the intravenous catheter and the extension tube being in fluid communication with the lumen;

a needle hub having a closed end, an open end, and a compartment interposed therebetween, the closed end being configured to receive a terminal end of the extension tube and the open end configured to receive the proximal end of the catheter adapter, wherein the extension tube is wound around a body of an introducer needle within the compartment; and

the introducer needle having a base end, a tip end, and the body extending therebetween, the base end being securely attached to the closed end of the needle hub, and the body extending through the proximal end of the catheter adapter, the lumen, the distal end of the catheter adapter, and the intravenous catheter such that the tip end of the introducer needle is exposed beyond a terminal end of the intravenous catheter.

2. The assembled intravenous catheter device ofclaim 1, wherein the proximal end of the catheter adapter further comprises a blood control valve, wherein the body of the introducer needle extends through the blood control valve.

3. The assembled intravenous catheter device ofclaim 2, wherein the blood control valve comprises a septum.

4. The assembled intravenous catheter device ofclaim 2, wherein the blood control valve comprises a self-sealing polymer.

5. The assembled intravenous catheter device ofclaim 1, further comprising a safety mechanism slidably coupled to the body of the introducer needle and configured to capture and retain the tip end of the introducer needle upon removal of the catheter adapter and the extension tube from the needle hub.

6. The assembled intravenous catheter device ofclaim 1, wherein a proximal end of the extension tube further comprises a blood control valve.

7. The assembled intravenous catheter device ofclaim 6, wherein the blood control valve further comprises a passageway, wherein the body of the introducer needle extends through the passageway.

8. The assembled intravenous catheter device ofclaim 6, wherein the blood control valve is a septum.

9. The assembled intravenous catheter device ofclaim 6, wherein the blood control valve is a self-sealing polymer.

10. The assembled intravenous catheter device ofclaim 6, wherein the blood control valve is a luer adapter.

11. The assembled intravenous catheter device ofclaim 1, wherein a gauge of the extension tube is greater than a gauge of the intravenous catheter.

12. The assembled intravenous catheter device ofclaim 1, wherein the securement platform comprises a pliable, flexible polymer material.

13. The assembled intravenous catheter device ofclaim 1, wherein the closed end of the needle hub further comprises a flashback chamber.

14. The assembled intravenous catheter device ofclaim 1, wherein a length of the extension tube is greater than a length of the compartment.

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